You Searched For: Trimethylamine+N-oxide


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Supplier: TCI America
Description: CAS Number: 1184-78-7 MDL Number: MFCD00002048 Molecular Formula: C3H9NO Molecular Weight: 75.11 Purity/Analysis Method: <gt/>95.0% (T) Form: Crystal Color: White Melting point (°C): 222
Supplier: Ambeed
Description: Trimethylamine oxide, Purity: 98%, CAS Number: 1184-78-7, Appearance: White to Very pale yellow Solid, Storage: Inert atmosphere, Room Temperature, Size: 25G

Supplier: Ambeed
Description: Trimethylamine oxide dihydrate, Purity: 98%, CAS number: 62637-93-8, Appearance: Form: powder Colour: white, Storage: Sealed in dry, Room Temperature, Size: 1000G

Catalog Number: (TCT0466-100G)
Supplier: TCI America
Description: CAS Number: 62637-93-8
MDL Number: MFCD00002048
Molecular Formula: C3H9NO
Molecular Weight: 75.11
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Color: White
Melting point (°C): 95

Supplier: BeanTown Chemical
Description: CAS: 62637-93-8; MDL No: MFCD00149077; RTECS: YH2850000 Crystalline; Linear Formula: (CH3)3NO·2H2O; MW: 111.14 Melting Point: 95-99°

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Catalog Number: (76577-220)
Supplier: AFG BIOSCIENCE LLC
Description: Human Trimethylamine-N-Oxide (TMAO) ELISA Kit, AFG Bioscience


Supplier: Thermo Scientific Chemicals
Description: Fieser: 1,1230 6,624 7,392 9,488 10,423 12,533 13,325 14,329 16,360
Catalog Number: (77511-022)
Supplier: AFG BIOSCIENCE LLC
Description: Mouse TMAO (Trimethylamine-N-oxide) ELISA Kit

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Catalog Number: (77525-880)
Supplier: AFG BIOSCIENCE LLC
Description: Human TMAO (Trimethylamine-N-oxide) ELISA Kit

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Catalog Number: (77526-498)
Supplier: AFG BIOSCIENCE LLC
Description: TMAO (Trimethylamine-N-oxide) ELISA Kit

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Catalog Number: (77695-256)
Supplier: LGC STANDARDS
Description: Trimethylamine-d9 N-Oxide, TRC, LGC Standards

New Product


Supplier: HiMedia
Description: TMAO (Trimethylamine-N-Oxide Medium) medium is used for the cultivation and differentiation of Campylobacter species from foods, except <i>C. jejuni </i>and <i>C. coli</i> in accordance with APHA.

Catalog Number: (10291-408)
Supplier: Bioss
Description: The Flavin containing monooxygenase family consists of five gene products, FMO1-5, that are major enzymatic oxidants involved in the metabolism of various therapeutics. Located in the liver, FMO3 is a hepatic microsomal enzyme that oxygenates soft nucleophiles such as secondary and tertiary amines. Through its N-oxygenase capabilities, FMO3 acts on a variety of xenobiotics to catalyze oxidative digestion. Defects in the FMO3 gene are the primary cause of trimethylaminuria (TMAuria), an inborn error of metabolism associated with a fishy body odor emitting from sweat, urine and breath. Genetic mutations in FMO3 lead to the N-oxidation of amino-trimethylamine derived from food products, thus producing the malodor associated with TMAuria.


Catalog Number: (10291-428)
Supplier: Bioss
Description: The Flavin containing monooxygenase family consists of five gene products, FMO1-5, that are major enzymatic oxidants involved in the metabolism of various therapeutics. Located in the liver, FMO3 is a hepatic microsomal enzyme that oxygenates soft nucleophiles such as secondary and tertiary amines. Through its N-oxygenase capabilities, FMO3 acts on a variety of xenobiotics to catalyze oxidative digestion. Defects in the FMO3 gene are the primary cause of trimethylaminuria (TMAuria), an inborn error of metabolism associated with a fishy body odor emitting from sweat, urine and breath. Genetic mutations in FMO3 lead to the N-oxidation of amino-trimethylamine derived from food products, thus producing the malodor associated with TMAuria.


Catalog Number: (10291-420)
Supplier: Bioss
Description: The Flavin containing monooxygenase family consists of five gene products, FMO1-5, that are major enzymatic oxidants involved in the metabolism of various therapeutics. Located in the liver, FMO3 is a hepatic microsomal enzyme that oxygenates soft nucleophiles such as secondary and tertiary amines. Through its N-oxygenase capabilities, FMO3 acts on a variety of xenobiotics to catalyze oxidative digestion. Defects in the FMO3 gene are the primary cause of trimethylaminuria (TMAuria), an inborn error of metabolism associated with a fishy body odor emitting from sweat, urine and breath. Genetic mutations in FMO3 lead to the N-oxidation of amino-trimethylamine derived from food products, thus producing the malodor associated with TMAuria.


Catalog Number: (10291-424)
Supplier: Bioss
Description: The Flavin containing monooxygenase family consists of five gene products, FMO1-5, that are major enzymatic oxidants involved in the metabolism of various therapeutics. Located in the liver, FMO3 is a hepatic microsomal enzyme that oxygenates soft nucleophiles such as secondary and tertiary amines. Through its N-oxygenase capabilities, FMO3 acts on a variety of xenobiotics to catalyze oxidative digestion. Defects in the FMO3 gene are the primary cause of trimethylaminuria (TMAuria), an inborn error of metabolism associated with a fishy body odor emitting from sweat, urine and breath. Genetic mutations in FMO3 lead to the N-oxidation of amino-trimethylamine derived from food products, thus producing the malodor associated with TMAuria.


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
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